Symbol Name ID |
Pofut1
protein O-fucosyltransferase 1 MGI:2153207 |
! | Indicates phenotype varies with strain background. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of the neck |
Disease(s) Associated with POFUT1 | |
Dowling-Degos disease |
Mouse Phenotypes | embryonic growth retardation |
decreased embryo size |
decreased birth body size |
epidermal cyst |
decreased body length |
decreased body size |
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Availability | Mouse Genotype | ||||||
Pofut1cax/Pofut1cax | ! | ||||||
Pofut1tm1.1Ysa/Pofut1tm1.1Ysa | |||||||
Pofut1tm1Pst/Pofut1tm1Pst | |||||||
Pofut1tm2Pst/Pofut1tm1Pst | |||||||
Pofut1tm2Pst/Pofut1tm2Pst Tg(MMTV-cre)1Mam/0 (conditional) |
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Pofut1tm2Pst/Pofut1tm1Pst Shhtm2(cre/ERT2)Cjt/Shh+ (conditional) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/30/2024 MGI 6.23 |
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